607-66-9

2-Hydroxy-4-methylquinoline Chemical Structure
607-66-9

Chemical Structure

2-Hydroxy-4-methylquinoline

  • CAS No.: 607-66-9
  • Formula:C10H9NO
  • Molecular Weight:159.19

IUPAC Name: 4-methylquinolin-2(1H)-one

InChIKey: APLVPBUBDFWWAD-UHFFFAOYSA-N

SMILES: O=C1C=C(C=2C=CC=CC2N1)C

Biological Activity: 2-Hydroxy-4-methylquinoline is a synthetic intermediate. 2-Hydroxy-4-methylquinoline is formed via cyclization of acetoacetanilide under the action of concentrated sulfuric acid through the Conrad-Limpach-Knorr synthesis. 2-Hydroxy-4-methylquinoline can be used in studies related to the synthesis of chemotherapeutic agents[1].

Cat. No. Product Name Purity Description Pricing
HY-W106109
2-Hydroxy-4-methylquinoline 2-Hydroxy-4-methylquinoline is a synthetic intermediate. 2-Hydroxy-4-methylquinoline is formed via cyclization of acetoacetanilide under the action of concentrated sulfuric acid through the Conrad-Limpach-Knorr synthesis. 2-Hydroxy-4-methylquinoline can be used in studies related to the synthesis of chemotherapeutic agents.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References